Chemoselective deprotection and deprotection with concomitant reduction of 1,3-dioxolanes, acetals and ketals using nickel boride-Reference-Cited by-同舟云学术

Chemoselective deprotection and deprotection with concomitant reduction of 1,3-dioxolanes, acetals and ketals using nickel boride

Published:2015 Issue:16 Volume:5 Page:12048-12051
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Khurana Jitender M.¹²³⁴,Dawra Kiran¹²³⁴,Sharma Purnima¹²³⁴

Affiliation:

1. Department of Chemistry

2. University of Delhi

3. Delhi-110007

4. India

Abstract

Reductive deprotection of 1,3-dioxolanes, acetals/ketals to the corresponding aldehydes/ketones and deprotection with reduction to the corresponding alcohols using nickel boride has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C4RA15404E

Reference29 articles.

1. P. G. M. Wuts and T. W.Greene, in Greene's Protective Groups in Organic Synthesis, Wiley, New York, 4th edn, 2006

2. Methods for the Preparation of Acetals from Alcohols or Oxiranes and Carbonyl Compounds

3. Protecting Group Strategies in Organic Synthesis

4. Cerium(IV)-Catalyzed Deprotection of Acetals and Ketals under Mildly Basic Conditions

5. Remarkably efficient deprotection of cyclic acetals and ketals

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